Diversity Candidate Research Supplement to Study Human Cell Models of Aging

研究人类衰老细胞模型的多样性候选研究补充

• 批准号: 10369737
• 负责人: GERALD SHADEL
• 金额: $ 16万
• 依托单位: SALK INSTITUTE FOR BIOLOGICAL STUDIES
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-30 至 2025-05-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10369737
• 关键词: Address; Advocate; Age; Aging; Anatomy; Animal Model; Artificial Intelligence; Basic Science; Biological; Biological Aging; Biological Markers; Biological Models; Biology of Aging; Cell Aging; Cell Communication; Cell model; Cells; Chronology; Clinical; Collaborations; Communication; Communities; Complement; Complex; Computer Models; Custom; Data Set; Development; Ensure; Environment; Environmental Exposure; Epigenetic Process; Event; Functional disorder; Gene Expression; Goals; Grant; Head; Heterogeneity; Human; Imaging Techniques; Imaging technology; Individual; Infrastructure; Institution; Intervention; Investigation; Knowledge; Leadership; Life; Location; Longevity; Measures; Mentors; Methods; Mission; Modality; Modeling; Molecular; Organoids; Pathologic; Pathology; Pathway interactions; Persons; Phenotype; Physiological; Pliability; Politics; Process; Protocols documentation; Research; Research Personnel; Resolution; Resources; Risk Factors; Role; Sampling; Services; Shock; System; Technology; Tissue Model; Tissues; Training; age related; career development; cell age; cell type; cellular imaging; cohort; computerized tools; disorder risk; epigenomics; functional decline; healthspan; human disease; human model; human tissue; imaging approach; innovation; interest; intervention effect; mathematical model; meetings; member; multiple omics; new technology; news; novel; outreach; personalized intervention; programs; research and development; single cell analysis; transcriptomics; virtual

PROJECT SUMMARY – Overall Since aging is the biggest risk factor of most human diseases and the overall functional decline in individuals, there is great interest in understanding its biological underpinnings, with the ultimate goal of increasing the number of healthy and productive years of human life (i.e., healthspan). Conserved mechanisms of aging and longevity have been identified via investigations into the basic biology of aging. These include studies in model organisms that have also shown that aging is pliable, opening the door for healthspan-promoting interventions. However, a major complicating factor that impedes our understanding of aging and our ability to intervene is the intrinsic and induced heterogeneity of the process. Distinct cell types have intrinsically different aging modalities, and even identical cell types age at different rates depending on physiological context or environmental exposures. These and other cellular heterogeneities (e.g., altered epigenetic states and gene expression) can drive tissue dysfunction and age-related pathology that ultimately impact healthspan and lifespan. Unravelling this complexity experimentally requires application of robust single-cell and imaging approaches to address the heterogeneity of cellular aging head-on, as well as computational and mathematical modelling approaches to illuminate aging networks and pathway interactions that involve known hallmarks of aging. Another major gap in aging research is the need for new and better human cell and tissue models to allow basic research directly relevant to human aging. Thus, the overarching premise of the proposed San Diego Nathan Shock Center (SD-NSC) is to create the requisite infrastructure to facilitate and promote the systematic study of cellular heterogeneity in aging and to provide novel cell and tissue models for basic human aging studies. The SD-NSC will establish cutting-edge Research Resource Cores focused on: 1) novel human cell and organoid models of aging, including from a unique human aging cohort that is annotated for physical and functional measures of biological age, 2) single-cell and high resolution -omics and imaging techniques, and 3) computational modelling of aging networks. The SD-NSC Research Resource Cores will provide scientific services to the NSC Network and the aging research community, and disseminate samples, datasets protocols, and computational tools. These resources will be complemented by a Research Development Core and Center outreach activities that will provide: 1) pilot grants and customized mentoring programs to encourage and support early-stage and established investigators new to aging research, 2) innovative in- person and virtual training in advanced methods and technologies to address cellular heterogeneity, and 3) intellectual leadership through novel programming to encourage collaboration and the dissemination of knowledge related to the basic biology of aging. The SD-NSC will bring together complementary expertise and resources from three renowned San Diego research Institutions with the common goal of understanding the role of cellular heterogeneity in aging to ultimately enable interventions to extend human healthspan.

项目概要-总体 由于衰老是大多数人类疾病和个体整体功能下降的最大风险因素， 人们对了解其生物学基础非常感兴趣，最终目标是增加 人类健康和有生产力的生命年数（即，healthspan）。衰老的保守机制， 通过对衰老的基本生物学的研究，已经确定了长寿。其中包括模型研究 这些生物也表明衰老是柔韧的，为促进健康的干预措施打开了大门。 然而，阻碍我们对衰老的理解和干预能力的一个主要复杂因素是 过程的内在和诱导异质性。不同的细胞类型具有本质上不同的老化 形态，甚至相同的细胞类型以不同的速度老化，这取决于生理环境或 环境暴露。这些和其他细胞异质性（例如，改变的表观遗传状态和基因 表达）可以驱动组织功能障碍和年龄相关的病理，最终影响健康寿命， 寿命要解开这种复杂性的实验需要应用强大的单细胞和成像 解决细胞老化的异质性的方法，以及计算和数学 建模方法，以阐明老化网络和途径相互作用，涉及已知的标志， 衰老衰老研究的另一个主要空白是需要新的和更好的人类细胞和组织模型， 允许进行与人类衰老直接相关的基础研究因此，拟议的San Diego Nathan Shock Center（SD-NSC）将创建必要的基础设施，以促进和促进 系统研究衰老过程中细胞异质性，并为基础人类研究提供新的细胞和组织模型 老化研究SD-NSC将建立尖端研究资源核心，重点关注：1）新人类 衰老的细胞和类器官模型，包括来自独特的人类衰老队列，该队列经过物理注释 和生物年龄的功能测量，2）单细胞和高分辨率组学和成像技术， 3）老化网络的计算建模。SD-NSC研究资源核心将提供 为NSC网络和老龄化研究界提供科学服务，并传播样本、数据集 协议和计算工具。这些资源将由研究开发核心补充 和中心的外展活动，将提供：1）试点赠款和定制的辅导计划， 鼓励和支持早期和成熟的研究人员新的老龄化研究，2）创新， 在先进的方法和技术方面进行人员和虚拟培训，以解决细胞异质性问题，以及3） 通过新颖的节目，鼓励合作和传播知识， 与衰老的基础生物学相关的知识。SD-NSC将汇集互补的专业知识， 来自三个著名的圣地亚哥研究机构的资源，其共同目标是了解 细胞异质性在衰老中的作用，最终使干预措施能够延长人类的健康寿命。